Quality Assurance Officer / Region Brussels / Permanent / € 2800 - € 3700 gross
Location: BelgiumSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Brussels Hoofdstedelijk Gewest Belgium.
• Returned Goods handling: To execute assessments of the product quality of returned goods and document accordingly.
• Quality system: To play an active role in the monitoring of the compliance of all activities on site and activities performed by subcontractors
• Customer care: Providing support to various internal and external customers.
• Re-packaging activities
• Knowledge of GMP and GDP
• Knowledge of quality management systems
• Problem-solver
• Communicative
• Excellent written and spoken French and English
• Be able to work individually and independently within a team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
The Company
Interesting client who is developing and build towards a better access to health for everyone.Role Description
In this role you will support the QA Manager and Quality team in the maintenance and improvement of quality standards, in line with regulatory and customer requirements. You will advise in the translation of GMP, GDP, ISO and customer requirements. You will support operations in the investigation of issues and advising for the corrective and preventive actions to prevent reoccurrence and participating in risk assessment exercises.Responsibilities
• Batch release: To prepare the dossiers needed by the delegated QP/RP for the release of products.• Returned Goods handling: To execute assessments of the product quality of returned goods and document accordingly.
• Quality system: To play an active role in the monitoring of the compliance of all activities on site and activities performed by subcontractors
• Customer care: Providing support to various internal and external customers.
• Re-packaging activities
Requirements
• Experience in Pharmaceutical Industry in a Quality role• Knowledge of GMP and GDP
• Knowledge of quality management systems
• Problem-solver
• Communicative
• Excellent written and spoken French and English
• Be able to work individually and independently within a team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
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